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首页> 外文期刊>Water Research >Pilot-scale evaluation of micropollutant abatements by conventional ozonation, UV/O_3, and an electro-peroxone process
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Pilot-scale evaluation of micropollutant abatements by conventional ozonation, UV/O_3, and an electro-peroxone process

机译:通过传统的臭氧氧化,UV / O_3和电过氧化物处理工艺对微污染物的减排进行中试评估

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摘要

The electro-peroxone (E-peroxone) process is an emerging ozone-based advanced oxidation process (AOP) that has shown large potential for micropollutant abatement in water treatment. To evaluate its performance under more realistic conditions of water treatment, a continuous-flow pilot E-peroxone system was developed and compared with conventional ozonation and a UV/O-3 process for micropollutant abatements in various water matrices (groundwater, surface water, and secondary wastewater effluent) in this study. With a specific ozone dose of 1.5 mg o(3)/mg DOC, micropollutants that have high and moderate reactivity with ozone (O-3) (diclofenac, naproxen, gemfibrozil, and bezafibrate) could be sufficiently abated (90% abatement) in the various waters by all three processes. However, ozoneresistant micropollutants (ibuprofen, clofibric acid, and chloramphenicol) were abated only by similar to 32 -68%, 68-91%, and 73-90% during conventional ozonation of the selected groundwater, surface water, and secondary wastewater effluent, respectively. By electro-generating H2O2 or applying UV irradiation to enhance o(3) transformation to center dot OH during ozonation, the E-peroxone and UV/O-3 processes similarly enhanced the abatement efficiencies of ozone-resistant micropollutants by similar to 15-43%, similar to 5-15%, and similar to 5 -10% in the groundwater, surface water, and secondary wastewater effluent, respectively. In addition, the E-peroxone and UV/O-3 processes significantly reduced bromate formation during the treatment of the three waters compared to conventional ozonation. Due to its higher efficiency, the E-peroxone process reduced similar to 10-53% of the energy consumption required to abate the concentration of chloramphenicol (the most ozone-resistant micropollutant spiked in the waters) by 1 order of magnitude in the three waters compared to conventional ozonation. In contrast, the UV/O-3 process consumed approximately 4 -10 times higher energy than conventional ozonation. This pilot-scale study demonstrates that the E-peroxone process can provide a feasible, effective, and energy-efficient alternative for micropollutant abatement and bromate control in water and wastewater treatment. (C) 2018 Elsevier Ltd. All rights reserved.
机译:电过氧化物(E-peroxone)工艺是一种新兴的基于臭氧的高级氧化工艺(AOP),在水处理中显示出巨大的微污染物减排潜力。为了评估其在更现实的水处理条件下的性能,开发了一种连续流先导E-过氧化物系统,并将其与传统的臭氧氧化和UV / O-3工艺进行了比较,以减少各种水基体(地下水,地表水和水)中的微污染物。二级废水)。使用1.5 mg o(3)/ mg DOC的特定臭氧剂量,可以充分减轻与臭氧(O-3)(双氯芬酸,萘普生,吉非贝齐和苯扎贝特)具有高和中等反应性的微污染物(减少90%以上)通过所有三个过程在各个水域中但是,在对选定的地下水,地表水和二次废水进行常规臭氧化过程中,耐臭氧的微污染物(布洛芬,氯纤维酸和氯霉素)的排放量仅减少了32%-68%,68-91%和73-90%,分别。通过电生成H2O2或施加UV辐射以增强臭氧化过程中o(3)向中心点OH的转化,E-过氧酮和UV / O-3工艺通过类似于15-43的方法提高了耐臭氧性微污染物的减排效率。分别在地下水,地表水和二次废水中所占百分比分别为5-15%和5 -10%。此外,与传统的臭氧化相比,E-过氧化物和UV / O-3工艺在三种水处理过程中显着减少了溴酸盐的形成。由于其较高的效率,E-peroxone工艺在三种水中将氯霉素(在水中加标的最耐臭氧的微污染物)的浓度降低了所需能量消耗的10-53%,降低了一个数量级。与传统的臭氧化相比相比之下,UV / O-3工艺消耗的能量比传统的臭氧化大约高4 -10倍。这项中试规模的研究表明,E-peroxone工艺可以为水和废水处理中的微污染物减排和溴酸盐控制提供可行,有效和节能的替代方案。 (C)2018 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Water Research》 |2018年第1期|106-117|共12页
  • 作者单位

    Tsinghua Univ, Beijing Key Lab Emerging Organ Contaminants Contr, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Con, Beijing 100084, Peoples R China;

    Tsinghua Univ, Beijing Key Lab Emerging Organ Contaminants Contr, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Con, Beijing 100084, Peoples R China;

    Tsinghua Univ, Beijing Key Lab Emerging Organ Contaminants Contr, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Con, Beijing 100084, Peoples R China;

    Tsinghua Univ, Beijing Key Lab Emerging Organ Contaminants Contr, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Con, Beijing 100084, Peoples R China;

    Tsinghua Univ, Beijing Key Lab Emerging Organ Contaminants Contr, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Con, Beijing 100084, Peoples R China;

    Tsinghua Univ, Beijing Key Lab Emerging Organ Contaminants Contr, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Con, Beijing 100084, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Advanced oxidation; Bromate; Emerging contaminant; Energy efficiency; Pharmaceutical; Water and wastewater treatment;

    机译:高级氧化;溴酸盐;新兴污染物;能效;制药;水和废水处理;

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